Truvic Medical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Truvic Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Campbell, US.
Last cleared in 2023. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Truvic Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Cardiomed Device Consultants and Cardiomed Devices Consultants.
FDA 510(k) Regulatory Record - Truvic Medical, Inc.
2 devices